Du verwaltest Proben und führst analytische Tests sowie Dokumentationen nach GxP-Standards durch. Außerdem meldest du technische Beschwerden schnell.
Anforderungen
- •Sound technical knowledge of pharmaceuticals
- •Working experience in laboratory environment
- •Continuous learning ability
- •Dealing with ambiguity
- •Decision-making skills
- •GxP knowledge
- •Understanding industry standards
- •Laboratory equipment proficiency
- •Commitment to laboratory excellence
- •Quality control testing knowledge
- •Quality control sampling skills
- •Self-awareness
- •Technological expertise
- •Total quality management knowledge
- •Fluent in English
Deine Aufgaben
- •Probenlagerung und -verwaltung
- •Analytische Tests und Dokumentation von Arzneimittel-, Fertigprodukt-, Beschwerde-, Stabilitäts- und Verpackungsmaterialproben nach GxP-Standards
- •Analytische Dokumentation von Stabilitätsproben nach GxP-Standards
- •Technische Beschwerden und unerwünschte Ereignisse innerhalb von 24 Stunden melden
- •Verteilung von Marketingproben (falls zutreffend)
Original Beschreibung
# QC Analyst II
**Stein Aargau** | **Full time**
**Job Description Summary**
-This role utilizes chemistry laboratory skills to test and measure product or materials while ensuring that analysis is performed according to established Standard Operating Procedures (SOPs), Analytical Methods & current Compendia.
**Job Description**
**Major accountabilities:**
* Sample storage and management -Analytical testing/documentation of drug product / finished product / complaints / stability / packaging material samples to GxP standards Stability -Testing/Sample storage and management .
* Analytical documentation of stability samples to GxP standards -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)
**Key performance indicators:**
* Orders are processed correctly and quickly.
* No waiting times due to wrong or delayed order.
* Deadline adherence rate: orders completed on time, all missed deadlines reported in good time, the shortest possible lead time -Ensure constant readiness for inspection, no critical complaints from superiors and inspectors -Consistently follow the GMP and GSU guidelines, as well as the SOPs, no critical irregularities -Finding and implementing optimization options to reduce costs -Completed training plan
**Minimum Requirements:**
**Work Experience:**
* Sound technical & scientific knowledge of pharmaceutical/ chemical.
* Working experience in Laboratory environment in the Pharmaceutical.
* analytics/QC/ equivalent.
* industry.
**Skills:**
* Continuous Learning.
* Dealing With Ambiguity.
* Decision Making Skills.
* Gxp.
* Industry Standards.
* Laboratory Equipment.
* Laboratory Excellence.
* Quality Control (Qc) Testing.
* Quality Control Sampling.
* Self Awareness.
* Technological Expertise.
* Total Quality Management.
**Languages :**
* English.
**Skills Desired**
Continued Learning, Dealing With Ambiguity, Decision Making Skills, Gxp, Industry Standards, Laboratory Equipment, Laboratory Excellence, Quality Control (Qc) Testing, Quality Control Sampling, Self-Awareness, Technological Expertise, Total Quality Management